C3149462[trait identifier] AND "Revvity Omics, Revvity"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1324061	NM_000078.3(CETP):c.160C>T (p.Arg54Ter)	CETP (R54*)	Single nucleotide variant (nonsense)	Hyperalphalipoproteinemia 1	GLikely pathogenic
Select item 2690563	NM_000078.3(CETP):c.266del (p.Ser89fs)	CETP (S89fs)	Deletion (frameshift variant)	Hyperalphalipoproteinemia 1	GLikely pathogenic
Select item 1322066	NM_000078.3(CETP):c.268C>T (p.Gln90Ter)	CETP (Q90*)	Single nucleotide variant (nonsense)	Hyperalphalipoproteinemia 1	GPathogenic
Select item 2439924	NM_000078.3(CETP):c.544C>T (p.Gln182Ter)	CETP (Q182*)	Single nucleotide variant (nonsense)	Hyperalphalipoproteinemia 1	GUncertain significance
Select item 2690564	NM_000078.3(CETP):c.964C>T (p.Gln322Ter)	CETP (Q262* +1 more)	Single nucleotide variant (nonsense)	Hyperalphalipoproteinemia 1	GLikely pathogenic
Select item 1324062	NM_000078.3(CETP):c.981+2T>C	CETP	Single nucleotide variant (splice donor variant)	Hyperalphalipoproteinemia 1	GLikely pathogenic
Select item 17524	NM_000078.3(CETP):c.1321+1G>A	CETP	Single nucleotide variant (splice donor variant)	Hyperalphalipoproteinemia 1	GPathogenic

ClinVar